Metabolic Flux and Growth Profiling of Megasphaera cerevisiae for Medium-Chain Fatty Acid Synthesis

IF 3.1 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Wael Sabra, Sonia Villotti, Joachim Fensterle, An-Ping Zeng, Ahmed M. Haddad
{"title":"Metabolic Flux and Growth Profiling of Megasphaera cerevisiae for Medium-Chain Fatty Acid Synthesis","authors":"Wael Sabra,&nbsp;Sonia Villotti,&nbsp;Joachim Fensterle,&nbsp;An-Ping Zeng,&nbsp;Ahmed M. Haddad","doi":"10.1111/1758-2229.70390","DOIUrl":null,"url":null,"abstract":"<p><i>Megasphaera cerevisiae</i> is a well-known beer spoilage organism, capable of producing undesirable flavours and turbidity. Although the biosynthesis of medium-chain fatty acids (MCFAs) has been extensively studied in different Megasphaera species, the metabolic behaviour of <i>M. cerevisiae</i> in controlled environments remains largely unexplored. This study examines the MCFAs production from diverse substrates and reports flux analyses of core metabolism for the first time using a genome-scale model. The results suggest that acetate stimulates butyrate production but not caproic acid production. Butyrate supplementation, either alone or in combination with acetate, promoted CA synthesis. Lactate supplementation primarily led to the formation of propionic acid and acetic acid. The metabolic network model was manually curated and validated against the different experimental data. The metabolic flux results showed that butyrate production facilitated via the reverse β-oxidation (RBO) pathway, with a minor contribution from the fatty acid synthesis (FAS) pathway. Conversely, CA synthesis was mainly synthesised through the FAS pathway, irrespective of the substrate used. The pathway analyses results highlighted the critical role of hydrogen production in <i>M. cerevisiae</i> metabolism, particularly under conditions where lactate is utilised. Collectively, these findings offer novel insights into the metabolic versatility and pathway preferences of <i>M. cerevisiae</i>.</p>","PeriodicalId":163,"journal":{"name":"Environmental Microbiology Reports","volume":"18 4","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2026-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13400456/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Microbiology Reports","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1758-2229.70390","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Megasphaera cerevisiae is a well-known beer spoilage organism, capable of producing undesirable flavours and turbidity. Although the biosynthesis of medium-chain fatty acids (MCFAs) has been extensively studied in different Megasphaera species, the metabolic behaviour of M. cerevisiae in controlled environments remains largely unexplored. This study examines the MCFAs production from diverse substrates and reports flux analyses of core metabolism for the first time using a genome-scale model. The results suggest that acetate stimulates butyrate production but not caproic acid production. Butyrate supplementation, either alone or in combination with acetate, promoted CA synthesis. Lactate supplementation primarily led to the formation of propionic acid and acetic acid. The metabolic network model was manually curated and validated against the different experimental data. The metabolic flux results showed that butyrate production facilitated via the reverse β-oxidation (RBO) pathway, with a minor contribution from the fatty acid synthesis (FAS) pathway. Conversely, CA synthesis was mainly synthesised through the FAS pathway, irrespective of the substrate used. The pathway analyses results highlighted the critical role of hydrogen production in M. cerevisiae metabolism, particularly under conditions where lactate is utilised. Collectively, these findings offer novel insights into the metabolic versatility and pathway preferences of M. cerevisiae.

Abstract Image

酵母中链脂肪酸合成的代谢通量和生长特征。
酿酒巨霉是一种众所周知的啤酒腐败菌,能够产生不良的味道和浑浊。虽然中链脂肪酸(MCFAs)的生物合成已经在不同的巨藻物种中得到了广泛的研究,但酿酒分枝杆菌在受控环境中的代谢行为仍然很大程度上未被探索。本研究研究了不同底物产生的MCFAs,并首次使用基因组尺度模型报道了核心代谢的通量分析。结果表明,乙酸刺激丁酸的产生,但不刺激己酸的产生。单独添加丁酸盐或与醋酸盐联合添加丁酸盐均能促进CA的合成。乳酸的补充主要导致丙酸和乙酸的形成。代谢网络模型是手工编制的,并根据不同的实验数据进行验证。代谢通量结果表明,丁酸盐的生成通过反向β-氧化(RBO)途径促进,脂肪酸合成(FAS)途径贡献较小。相反,CA合成主要通过FAS途径合成,而不考虑使用的底物。途径分析结果强调了产氢在酿酒酵母代谢中的关键作用,特别是在乳酸被利用的条件下。总的来说,这些发现为酿酒分枝杆菌的代谢多样性和途径偏好提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书